Variant #0000284740 (NC_000001.10:g.1735935T>C, NM_002074.3:c.353A>G (GNB1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1735935T>C |
| DNA change (hg38) |
g.1804496T>C |
| Published as |
GNB1(NM_002074.3):c.353A>G (p.(Asp118Gly)), GNB1(NM_002074.5):c.353A>G (p.D118G) |
| ISCN |
- |
| DB-ID |
GNB1_000012 See all 2 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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